Publications by authors named "Israel Schechter"

Multiphoton electron extraction spectroscopy (MEES) is an advanced analytical technique that has demonstrated exceptional sensitivity and specificity for detecting molecular traces on solid and liquid surfaces. Building upon the solid-state MEES foundations, this study introduces the first application of MEES in the gas phase (gas-phase MEES), specifically designed for quantitative detection of gas traces at sub-part per billion (sub-PPB) concentrations under ambient atmospheric conditions. Our experimental setup utilizes resonant multiphoton ionization processes using ns laser pulses under a high electrical field.

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The development of rapid methods for the detection of virus particles based on their intrinsic fluorescence (the native auto-fluorescence that originates from the non-labeled analyte) is challenging. Pure viruses may be detected in filtered solutions, based on the strong fluorescence of the amino acid tryptophan (Trp) in their proteins. Nevertheless, Trp also exists in high quantities in the hosts and host cultivation media.

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Human health is consistently threatened by different species of pathogenic bacteria. To fight the spread of diseases, it is important to develop rapid methods for bacterial identification. Over the years, different kinds of biosensors were developed for this cause.

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Fast identification of pathogenic bacteria is an essential need for patient's diagnostic in hospitals and environmental monitoring of water and air quality. Bacterial cells consist of a very high amount of biological molecules whose content changes in response to different environmental conditions. The similarity between the molecular compositions of different bacterial cells limits the possibility to find unique markers to enable differentiation among species.

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Multiphoton electron extraction spectroscopy (MEES) is an analytical method for direct analysis of solids under ambient conditions in which the samples are irradiated by short UV laser pulses and the photocharges emitted are recorded as a function of the laser wavelength. The method is very sensitive, and many peaks are observed at wavelengths that are in resonance with the surface molecules. The analytical capabilities of MEES have recently been demonstrated, and here we perform a systematic comparison with some traditional spectroscopies that are commonly applied to material analysis.

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Multiphoton electron extraction spectroscopy (MEES) is an analytical method in which UV laser pulses are utilized for extracting electrons from solid surfaces in multiphoton processes under ambient conditions. Counting the emitted electrons as a function of laser wavelength results in detailed spectral features, which can be used for material identification. The method has been applied to detection of trace explosives on a variety of surfaces.

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The properties of biomaterials, including their surface microstructural topography and their surface chemistry or surface energy/wettability, affect cellular responses such as cell adhesion, proliferation, and migration. The nanotopography of moderately rough implant surfaces enhances the production of biological mediators in the peri-implant microenvironment with consequent recruitment of differentiating osteogenic cells to the implant surface and stimulates osteogenic maturation. Implant surfaces with moderately rough topography and with high surface energy promote osteogenesis, increase the ratio of bone-to-implant contact, and increase the bonding strength of the bone to the implant at the interface.

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Endosteal dental implants are used routinely with high success rates to rehabilitate the integrity of the dentition. However if implant surfaces become contaminated by foreign material, osseointegration may not occur and the dental implant will fail because of the lack of mechanical stability. Detection and characterization of dental implant surface contaminants is a difficult task.

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An optical analytical method, based on complexation reactions of organic azo-dyes with heavy metals, is proposed. It is based on a specially designed polymeric film that when submerged in water contaminated with heavy metals it changes its color. The azo-dyes are injected into the tested water, resulting in formation of nano-particles of insoluble complexes.

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Our previously reported computational study of the decomposition pathways of triacetone triperoxide (TATP), 1, predicted that unlike most energetic materials, which involve self-combustion of fuel and oxidants, 1 decomposes via a thermoneutral, non-redox pathway that involves entropy burst. These predictions are now corroborated by time-resolved monitoring of deflagration or detonation of 1 using a fast video camera following initiation by a short pulse focused laser beam. While a fireball always accompanies the explosion of 1 under air, the formation of a fireball is totally prevented under a nitrogen atmosphere.

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β-site APP-cleaving enzyme (BACE1) cleaves the wild type (WT) β-site very slowly (k(cat)/K(m): 46.6 m(-1) s(-1)). Therefore we searched for additional β-secretases and identified three cathepsins that split the WT β-site much faster.

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Various metals undergo complexation with organic reagents, resulting in colored products. In practice, their molar absorptivities allow for quantification in the ppm range. However, a proper pre-concentration of the colored complex on paper filter lowers the quantification limit to the low ppb range.

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Direct detection of solid substances is an important yet challenging issue in analytical chemistry. Laser multiphoton ionization spectroscopy has been applied for the first time for direct analysis of solids under ambient conditions. In this method, a solid powder/film is placed on a conductive surface and is irradiated by a pulsed tunable laser while an electrical field of approximately 2 kV cm(-1) is applied across this conductive surface and another electrode.

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A nondestructive method for quantitative parchment characterization and sensitive indication of its deterioration stage was developed. Synchronous fluorescence (SF) measurements were applied for the first time to parchment samples. The method provides detailed spectral features, which are useful for parchment characterization.

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This highlight article describes three Alzheimer's disease (AD) studies presented at the 5th General Meeting of the International Proteolysis Society that address enzymatic mechanisms for producing neurotoxic beta-amyloid (Abeta) peptides. One group described the poor kinetics of BACE 1 for cleaving the wild-type (WT) beta-secretase site of APP found in most AD patients. They showed that cathepsin D displays BACE 1-like specificity and cathepsin D is 280-fold more abundant in human brain than BACE 1.

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Many studies suggest that BACE 1 is the genuine beta-secretase; however, this is not undisputed. The wild-type (WT) beta-site of the amyloid precursor protein (APP) present in the worldwide population is cleaved very slowly (kcat/Km: approx. 50 m(-1) s(-1)), while proteases acting on relevant substrates are much more efficient (kcat/Km: 10(4)-10(6) m(-1) s(-1)).

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A non-destructive and non-invasive method for quantitative characterization of parchment deterioration, based on spectral measurements, is proposed. Deterioration due to both natural aging (ancient parchments) and artificial aging (achieved by means of controlled UV irradiation and temperature treatment) was investigated. The effect of aging on parchment native fluorescence was correlated with its deterioration condition.

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This study addresses the necessity to provide fast assessment of pesticide coverage on plants, which is required for saving the expensive compounds and for protecting the environment against overdosing. The feasibility of applying several optical methods for direct detection of the pesticides on plants has been investigated. In order to overcome the matrix effect, which is related to plant fluorescence emission and to physiological spectral interferences, we suggest the application of a fluorescent labeling agent, in form of nano- and micro-crystallites.

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Competitive inhibitors can activate proteases (papain, trypsin, and cathepsin S) to catalyze the synthesis of peptide bonds and accelerate the hydrolysis of poor substrates (from 1 to 99%). Reaction mixtures contained intermediate molecules that were formed by the coupling of the inhibitor with the poor substrate. This and other findings suggest the following chain of events.

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Parchment from different sources has been analyzed by laser-induced breakdown spectroscopy (LIBS) for determination of Ca, Na, K, Mg, Fe, Cu, and Mn. The LIBS results were compared with results from inductively coupled plasma spectroscopy (ICP) and good correlation was obtained. Rapid distinction between modern and historical samples was achieved by discriminant analysis of the LIBS data.

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Nonresonant cavity ringdown laser absorption spectroscopy (CRLAS) was applied for detection and characterization of airborne particulates. Sensitive detection of a variety of aerosols under ambient conditions was achieved. The method provides, for the first time, time-resolved absolute aerosol concentration, with spatial resolution (along a line).

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Laser-induced breakdown spectroscopy (LIBS) has been used to map the distribution of particulate matter inside the plume created by laser ablation of a brass target. The spatial density distribution of the different components of the plume was determined in an attempt to reveal the mechanism of fractionation in the process of the laser ablation. In this experiment two Nd:YAG pulsed lasers were used.

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The application of finely divided (black) Pd and Pd-Fe powder in the sono-electro-catalytic reduction of chlorophenoxy herbicides (2,4-D) and chlorophenols (2,4-DCP) in aqueous solutions allows for effective destruction of toxic chlorinated aromatic compounds. At 20 degrees C complete conversion of these compounds is observed within 10 min. On bimetallic Pd/Fe catalyst, intermediates due to the oxidation reaction are detected in addition to the products of dechlorination.

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It is estimated that most polycyclic aromatic hydrocarbons (PAHs) in environmental water are not dissolved but rather in particulate form. Nevertheless, the currently available optical detectors are not suited for proper sampling of solid PAHs. A new setup for direct sampling and quantification of suspended particulate PAHs in water is suggested.

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